반응 #607953

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aminophenol

Boc-Tle-OH

→

2h

(S)-2-((3-(tert-Butyl)-2-hydroxybenzyl)amino)-N,N,3,3-tetramethylbutanamide

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후처리

1. 1
   기타The title compound is prepared
2. 2
   기타2) The product from the reduction process is quenched with a saturated solution of aqueous NaHCO3 (formation of the HCl salt
3. 3
   기타is purified by silica gel chromatography (9:1 hexanes:ethyl acetate to 6:1 hexanes:ethyl acetate to 4:1 hexanes:ethyl acetate)

실험 절차

The title compound is prepared according to the representative synthesis of aminophenol 2g except for the following changes: 1) Initial amide formation carried out with Boc-Tle-OH instead of Boc-Val-OH. 2) The product from the reduction process is quenched with a saturated solution of aqueous NaHCO3 (formation of the HCl salt is omitted) and the desired product is purified by silica gel chromatography (9:1 hexanes:ethyl acetate to 6:1 hexanes:ethyl acetate to 4:1 hexanes:ethyl acetate) to afford 2h as a white solid. M.p.=96-98° C. IR (neat): 2948 (w, br), 1639 (s), 1460 (m), 1433 (m), 1352 (m), 1240 (m), 1135 (m), 878 (m), 782 (m), 751 (s) cm−1; 1H NMR (400 MHz, CDCl3): δ 10.87 (1H, br s), 7.19 (1H, d, J=7.3 Hz), 6.77 (1H, d, J=7.3 Hz), 6.70 (1H, t, J=7.5), 4.09 and 3.40 (2H, ABq, JAB=13.6 Hz), 3.31 (1H, d, J=11.3 Hz), 3.03 (3H, s), 2.89 (3H, s), 2.71 (1H, br s), 1.40 (9H, s), 0.96 (9H, s); 13C NMR (100 MHz, CDCl3): δ 173.3, 157.0, 137.2, 126.9, 126.3, 122.9, 118.5, 62.4, 51.3, 38.0, 35.8, 34.8, 34.7, 29.6, 27.0; HRMS Calcd for C19H33N2O2 [M+H]+: 321.25420. Found: 321.25442. [α]20D=−33 (c=0.93, CHCl3).

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